AccessGUDID - DEVICE: Integrated Medical Specialties (10868564000051)

GUDID

Device Identifier (DI) Information

Brand Name: Integrated Medical Specialties
Version or Model: IMS044G
Commercial Distribution Status: In Commercial Distribution
Catalog Number:
Company Name: INTEGRATED MEDICAL SYSTEMS, INC.

Primary DI Number: 10868564000051
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 40
Labeler D-U-N-S® Number*: 962364444 *Terms of Use

Device Description: IV ADMIN SET, W/ GVS EASYDROP® FLOW REGULATOR,, 0.22µ IN LINE GVS SPEEDFLOW® AIR-ELIMINATING FILTER, DEHP-FREE, 1 Y-SITE, 15µ FILTER IN DRIP CHAMBER, SWIVEL LL, 92"

Device Characteristics

What MRI safety information does the labeling contain?	Labeling does not contain MRI Safety Information
Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437):	No
Device labeled as "Not made with natural rubber latex":	No
For Single-Use:	Yes
Prescription Use (Rx):	No
Over the Counter (OTC):	No
Kit:	No
Combination Product:	No
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P):	No

GMDN

[?]

GMDN Term Code	GMDN Term Name	GMDN Term Definition	GMDN Term Status [?]	Implantable?
58977	Basic intravenous administration set, noninvasive	A collection of noninvasive devices intended to conduct fluids from an intravenous (IV) administration bag/bottle to a peripheral venous cannula (not included) during gravitational or pump administration to a patient's venous system; some types may in addition be intended for enteral feeding applications. It typically includes tubing, connectors, chambers, and clamps; the bag/bottle may be included. It neither includes devices intended for invasive use nor a heat exchanger. This is a single-use device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
FPA	Set, Administration, Intravascular

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
Premarket Submission Number Not Available/Not Released

Device Exempt from Premarket Submission: No CLOSE

Sterilization

Device Packaged as Sterile: Yes
Requires Sterilization Prior to Use: No

Sterilization Method [?]
No Sterilization Methods Found

Storage and Handling

[?]

Storage and Handling
No storage/handling found

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: dd7f4a81-5e77-414f-a85d-892069da9233
Public Version Date: April 07, 2021
Public Version Number: 4
DI Record Publish Date: March 17, 2017